ライフサイエンスコーパス: Pan troglodytes

1 anual task were assessed in 109 chimpanzees (Pan troglodytes).

2 ologues in the MHC of the common chimpanzee (Pan troglodytes).

3 Homo sapiens) donors and common chimpanzees (Pan troglodytes).

4 of hand use in a sample of 187 chimpanzees (Pan troglodytes).

5 e was tested in a sample of 188 chimpanzees (Pan troglodytes).

6 ion was examined in 115 captive chimpanzees (Pan troglodytes).

7 tamarins (Saguinus mystax) and chimpanzees (Pan troglodytes).

8 uman brain, are also present in chimpanzees (Pan troglodytes).

9 area 10) cortices of developing chimpanzees (Pan troglodytes).

10 red helical filaments in an aged chimpanzee (Pan troglodytes).

11 llum from MRI brain scans of 53 chimpanzees (Pan troglodytes).

12 and maternal space use) in wild chimpanzees (Pan troglodytes).

13 ves, bonobos (Pan paniscus) and chimpanzees (Pan troglodytes).

14 our closest living relative, the chimpanzee (Pan troglodytes).

15 odeficiency virus (SIVcpz) from chimpanzees (Pan troglodytes).

16 pal and amygdalar volumes of 60 chimpanzees (Pan troglodytes).

17 mans in comparison to the common chimpanzee (Pan troglodytes).

18 precentral gyrus-morphology in chimpanzees (Pan troglodytes).

19 o and are significantly larger than those of Pan troglodytes.

20 (TCRBV) repertoire of the common chimpanzee Pan troglodytes.

21 olive baboon [Papio anubis]), 3 chimpanzees (Pan troglodytes), 6 members of the parrot (Psittacinae)

22 mpared among a group of 4 adult chimpanzees (Pan troglodytes), a group of 2 adult orangutans (Pongo p

23 In chimpanzees (Pan troglodytes), adult males are more gregarious than f

24 In three experiments, chimpanzees (Pan troglodytes) always chose between an option deliveri

25 In a series of experiments, chimpanzees (Pan troglodytes), an orangutan (Pongo pygmaeus), and hum

26 ure of the actively transcribed GLTP gene in Pan troglodytes and establish the intronless GLTP as a p

27 egies used to combine seriated cups by apes (Pan troglodytes and P. paniscus) and monkeys (Cebus apel

28 ata are available for our closest relatives, Pan troglodytes and Pan paniscus, data from the nonrecom

29 Observations of chimpanzees (Pan troglodytes) and bonobos (Pan paniscus) provide valu

30 mans' closest living relatives, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus), with a dyad

31 closest phylogenetic relatives, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus).

32 arative studies between humans, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus).

33 k was used to determine whether chimpanzees (Pan troglodytes) and children (Homo sapiens) who observe

34 In chimpanzees (Pan troglodytes) and common marmosets (Callithrix jacchu

35 in the genomes of 20 wild-born chimpanzees (Pan troglodytes) and have compared the identified chimpa

36 Here we tested chimpanzees (Pan troglodytes) and human children on a modified ultima

37 eixidor, and K. A. Bard tested chimpanzees' (Pan troglodytes) and human children's (Homo sapiens) ski

38 milarity between BT displays of chimpanzees (Pan troglodytes) and human smiles varied in relation to

39 identify a homologous region in chimpanzees (Pan troglodytes) and humans (Homo sapiens).

40 In this study, chimpanzees (Pan troglodytes) and orangutans (Pongo abelii) either ha

41 L1HS72) that was also present in the common (Pan troglodytes) and pygmy (P. paniscus) chimpanzee geno

42 ologues described to date in the chimpanzee (Pan troglodytes) and the four homologues described in ma

43 nzees (Pan paniscus), 13 common chimpanzees (Pan troglodytes) and three Hylobatidae (one Hylobates la

44 e found Plasmodium infection in chimpanzees (Pan troglodytes) and western gorillas (Gorilla gorilla),

45 orangutans (Pongo pygmaeus), 14 chimpanzees (Pan troglodytes), and 4 bonobos (Pan paniscus).

46 in 2- and 3-year-old children, chimpanzees (Pan troglodytes), and orangutans (Pongo pygmaeus).

47 Humans (Homo sapiens), chimpanzees (Pan troglodytes), and rhesus monkeys (Macaca mulatta) co

48 ter than that between the common chimpanzee, Pan troglodytes, and the pygmy chimpanzee or bonobo, Pan

49 Chimpanzees (Pan troglodytes) are often divided into subspecies, but

50 hypothesized to be homologous to chimpanzee (Pan troglodytes) border patrols.

51 ve been isolated from the common chimpanzee (Pan troglodytes), but only three such SIVcpz infections

52 ample of 80 preserved postmortem chimpanzee (Pan troglodytes) cerebral hemispheres.

53 five primate species, Homo sapiens (human), Pan troglodytes (chimpanzee), Papio hamadryas (baboon),

54 m Old World apes; Gorilla gorilla (gorilla), Pan troglodytes (chimpanzee), Pongo pygmaeus (orang-utan

55 nstitution of these two archaic hominins and Pan troglodytes (chimpanzee).

56 We have sequenced the Pan troglodytes class I (Patr) molecules from three comm

57 nera, Homo (Homo) sapiens (humankind), Homo (Pan) troglodytes (common chimpanzee), and Homo (Pan) pan

58 nzee research sites, we sampled a further 34 Pan troglodytes communities.

59 lthough this fossil is comparable in size to Pan troglodytes, computerized tomography scans of the ne

60 d since infancy, pairs of adult chimpanzees (Pan troglodytes) could trade between themselves to obtai

61 mans' closest living relatives, chimpanzees (Pan troglodytes), could punish an individual who stole f

62 Data from three African field sites on Pan troglodytes demonstrate an unambiguous pattern of a

63 t has been reported that common chimpanzees (Pan troglodytes) differ from humans in being capable of

64 Male chimpanzees, Pan troglodytes, differ from males in most other mammali

65 n-human primates, and show that chimpanzees (Pan troglodytes) do not take advantage of opportunities

66 controversial, particularly for chimpanzees (Pan troglodytes), for which it is difficult to rule out

67 conspecific face recognition in chimpanzees (Pan troglodytes) from 2 primate centers that provided di

68 e display from a cDNA library of chimpanzee (Pan troglodytes) gamma1/kappa antibody genes.

69 sess the referential function of chimpanzee (Pan troglodytes) gestures to obtain food.

70 uman equivalent chromosome(s) of chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla) and oranguta

71 Our study investigated Macaca mulatta, Pan troglodytes, Gorilla gorilla, and Homo sapiens haplo

72 in all four great ape species (Pan paniscus, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus) by var

73 s on joint attention in 4 great ape species (Pan troglodytes, Gorilla gorilla, Pongo spp., and Pan pa

74 lla (Gorilla gorilla) and common chimpanzee (Pan troglodytes) habitats in East and West Africa, the r

75 Two chimpanzees (Pan troglodytes) had a direct view of an experimenter pl

76 pygmaeus) and were compared with chimpanzee (Pan troglodytes) hand preferences in subjects that were

77 sing number of field studies of chimpanzees (Pan troglodytes) have achieved long-term status across A

78 Chimpanzees (Pan troglodytes) have been known to exhibit rudimentary

79 Captive chimpanzees (Pan troglodytes) have been shown to learn the use of nov

80 , however, researchers studying chimpanzees (Pan troglodytes) have challenged this idea.

81 Even though recent studies in chimpanzees (Pan troglodytes) have demonstrated population-level righ

82 NCE STATEMENT Recent studies in chimpanzees (Pan troglodytes) have shown that some can learn to produ

83 Common chimpanzees (Pan troglodytes) infected with hepatitis C virus (HCV) s

84 irus (SIVcpz) infection of wild chimpanzees (Pan troglodytes) is incomplete since few isolates, mostl

85 hereas our closest relative, the chimpanzee (Pan troglodytes), is often characterized as overly compe

86 ne of our closest relatives, the chimpanzee (Pan troglodytes), is viewed as a reluctant altruist, act

87 Whereas mammals (Pan troglodytes, Macaca mulatta, Rattus norvegicus, and

88 Two chimpanzees (Pan troglodytes) made numerousness judgments of nonvisib

89 mosomes of human (Homo sapiens), chimpanzee (Pan troglodytes), mouse (Mus musculus) and rat (Rattus n

90 phere dominance, in three great ape species (Pan troglodytes, Pan paniscus and Gorilla gorilla).

91 to human alleles, we sequenced 18 different Pan troglodytes (Patr) alleles of 14 chimpanzees, 2 of t

92 e characterized CD4+ T cells targeting seven Pan troglodytes (Patr) class II-restricted epitopes duri

93 ects of modified procedures on chimpanzees' (Pan troglodytes) performance in a scale model comprehens

94 locations in the chromosomes of chimpanzee (Pan troglodytes, PTR), gorilla (Gorilla gorilla, GGO) an

95 s investigated whether juvenile chimpanzees (Pan troglodytes) recognize and use enforced statistical

96 lence study of SIVcpz infection in five wild Pan troglodytes schweinfurthii communities in east Afric

97 ng several communities of chimpanzees of the Pan troglodytes schweinfurthii subspecies in Uganda.

98 eat ape vocal communication, the chimpanzee (Pan troglodytes schweinfurthii) 'pant hoot'.

99 nk trajectories in wild eastern chimpanzees (Pan troglodytes schweinfurthii) and find remarkable sex

100 Chimpanzees in east Africa (Pan troglodytes schweinfurthii) are also infected with S

101 d genetic data from the Kasekela chimpanzee (Pan troglodytes schweinfurthii) community in Gombe Natio

102 Vcpz sequence (TAN1) from a wild chimpanzee (Pan troglodytes schweinfurthii) from Gombe National Park

103 photographic study of subadult chimpanzees (Pan troglodytes schweinfurthii) in Kanyawara, Kibale Nat

104 cted from nonhabituated eastern chimpanzees (Pan troglodytes schweinfurthii) in the Issa Valley (n =

105 two neighbouring communities of chimpanzees (Pan troglodytes schweinfurthii) in the Kalinzu Forest, U

106 ing quality (body size) in wild chimpanzees (Pan troglodytes schweinfurthii), a species with long per

107 ans, bonobos (Pan paniscus) and chimpanzees (Pan troglodytes), share many traits that are common in h

108 uthors previously reported that chimpanzees (Pan troglodytes) showed a striking bias to select the la

109 of 4 originally cross-fostered chimpanzees (Pan troglodytes), still living freely, but now in a labo

110 n our closest living relatives, chimpanzees (Pan troglodytes), suggest that among primates, regular i

111 An 11-year-old female chimpanzee (Pan troglodytes) that had already learned a large number

112 4 was based on the finding that chimpanzees (Pan troglodytes) that have been trained on the concept o

113 We tested a chimpanzee (Pan troglodytes) that recognizes 128 spoken words, askin

114 Here we show that in Pan troglodytes the peak in root growth rate coincides w

115 hologous sequences in the common chimpanzee (Pan troglodytes ), the gorilla (Gorilla gorilla) and the

116 asure of psychopathy for use in chimpanzees (Pan troglodytes), the Chimpanzee Psychopathy Measure (CP

117 ted the inferior pulvinar of the chimpanzee (Pan troglodytes), the closest evolutionary relative of h

118 ocedure originally designed for chimpanzees (Pan troglodytes) to measure the reactions of Asian eleph

119 died experimentally by allowing chimpanzees (Pan troglodytes) to observe alternative patterns of acti

120 The ability of chimpanzees (Pan troglodytes) to recognize the correspondence between

121 d CC morphology from MRIs in 67 chimpanzees (Pan troglodytes) to see whether similar effects were pre

122 nhuman primate species, such as chimpanzees (Pan troglodytes), to a limited degree.

123 with bonobos (Pan paniscus) and chimpanzees (Pan troglodytes) (Total n = 119) to assess their motivat

124 Chimpanzees in west central Africa (Pan troglodytes troglodytes) are endemically infected wi

125 rains from west central African chimpanzees (Pan troglodytes troglodytes) but human viruses belonging

126 n this study, we show that wild chimpanzees (Pan troglodytes troglodytes) in the Goualougo Triangle t

127 valence in west central African chimpanzees (Pan troglodytes troglodytes) remain to be elucidated.

128 SIVcpz) from naturally infected chimpanzees (Pan troglodytes troglodytes) to man.

129 captive members of the chimpanzee subspecies Pan troglodytes troglodytes.

130 at eating among wild adult male chimpanzees (Pan troglodytes verus) in Tai National Park, Cote d'Ivoi

131 sult in the extirpation of local chimpanzee (Pan troglodytes verus) populations.

132 ool use comes from three Western chimpanzee (Pan troglodytes verus) sites in Cote d'Ivoire, aged betw

133 her a ripe-fruit specialist, the chimpanzee (Pan troglodytes verus), arrived earlier at breakfast sit

134 nine-member pedigree of Western chimpanzees, Pan troglodytes verus.

135 t sequence data from 10 Western chimpanzees, Pan troglodytes verus.

136 red as infants in Reno, Nevada, chimpanzees (Pan troglodytes) Washoe, Moja, Tatu, and Dar freely conv

137 000 conflict interactions in 44 chimpanzees (Pan troglodytes), we provide evidence for relatively sta

138 and numerousness judgments by 2 chimpanzees (Pan troglodytes) were investigated when 2 quantities of

139 Six chimpanzees (Pan troglodytes) were presented with pairs of color phot

140 osely related species (i.e. Homo sapiens and Pan troglodytes) where gene-specific clustering is evide

141 pointing in 3 adult, laboratory chimpanzees (Pan troglodytes) who have not received language training

142 rived from the liver of a common chimpanzee (Pan troglodytes) with hepatitis C, specifically recogniz

143 n liver biopsy specimens of two chimpanzees (Pan troglodytes) with previously resolved HCV infection